Evidence map›Paper›PMID 33064772›Full record

ArticlePLoS pathogens2020

The NS1 protein of the parvovirus MVM Aids in the localization of the viral genome to cellular sites of DNA damage.

Kinjal Majumder, Maria Boftsi, Fawn B Whittle, Juexin Wang, Matthew S Fuller, Trupti Joshi, David J Pintel

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 39 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Kinjal MajumderDepartment of Molecular Microbiology and Immunology, University of Missouri School of Medicine, Columbia, Missouri, United States of America.ORCID 0000-0002-1898-8251
Maria BoftsiChristopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, United States of America.
Fawn B WhittleDepartment of Molecular Microbiology and Immunology, University of Missouri School of Medicine, Columbia, Missouri, United States of America.
Juexin WangChristopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, United States of America.ORCID 0000-0002-2260-4310
Matthew S FullerUltragenyx Gene Therapy, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-4704-572X
Trupti JoshiChristopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, United States of America.ORCID 0000-0001-8944-4924
David J PintelDepartment of Molecular Microbiology and Immunology, University of Missouri School of Medicine, Columbia, Missouri, United States of America.ORCID 0000-0002-9959-2848
University of Missouri · USUltragenyx Pharmaceutical (United States) · USUniversity of Missouri Health System · US

Funding

Parvovirus RNA Processing and Gene Expression StrategiesR01AI046458 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI PINTEL, DAVID J. · 2000 to 2018
$4.6M
The parvovirus-induced DNA damage response and cell cycle perturbationsR01AI116595 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI PINTEL, DAVID J. · 2016 to 2020
$1.9M
How does a viral pathogen manipulate DNA Damage Responses to promote infection?R00AI148511 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI MAJUMDER, KINJAL · 2022 to 2023
$498k
Parvovirus RNA Processing and Gene Expression StrategiesR56AI046458 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI PINTEL, DAVID J. · 2013 to 2013
$374k
How does a viral pathogen manipulate the DNA Damage Response to promote successful viral infection?K99AI148511 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI MAJUMDER, KINJAL · 2020 to 2021
$207k
Interaction between parvovirus replication and the cellular DNA-damage responseF32AI131468 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI MAJUMDER, KINJAL · 2018 to 2020
$171k
NIAID NIH HHS F32 AI131468NIAID NIH HHS K99 AI148511NIAID NIH HHS R00 AI148511NIAID NIH HHS R01 AI046458NIAID NIH HHS R01 AI116595NIAID NIH HHS R56 AI046458
6 · The paper itself

Abstract

The autonomous parvovirus Minute Virus of Mice (MVM) localizes to cellular DNA damage sites to establish and sustain viral replication centers, which can be visualized by focal deposition of the essential MVM non-structural phosphoprotein NS1. How such foci are established remains unknown. Here, we show that NS1 localized to cellular sites of DNA damage independently of its ability to covalently bind the 5' end of the viral genome, or its consensus DNA binding sequence. Many of these sites were identical to those occupied by virus during infection. However, localization of the MVM genome to DNA damage sites occurred only when wild-type NS1, but not its DNA-binding mutant was expressed. Additionally, wild-type NS1, but not its DNA binding mutant, could localize a heterologous DNA molecule containing the NS1 binding sequence to DNA damage sites. These findings suggest that NS1 may function as a bridging molecule, helping the MVM genome localize to cellular DNA damage sites to facilitate ongoing virus replication.

Indexed as

DNA DamageAnimalsCell LineDNA-Binding ProteinsDNA ReplicationDNA, ViralFemaleGenome, ViralHumansMaleMiceMinute Virus of MiceParvoviridae InfectionsParvovirusViral Nonstructural ProteinsVirus ReplicationDNA-Binding ProteinsDNA, ViralNS1 protein, minute virus of miceViral Nonstructural Proteins

Identifiers

PMID33064772
PMCPMC7592911
OpenAlexW3093030757

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.